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Human Genetics

, Volume 89, Issue 1, pp 122–122 | Cite as

A rare MspI RFLP of the DMD probe p20 (DXS269)

  • S. Uhlhaas
  • E. Bakker
  • C. van Broeckhoven
  • A. Barth-Schulz
  • W. Friedl
DNA Variants
  • 26 Downloads

Summary

A rare polymorphism of the probe p20 in the Duchenne muscular dystrophy gene is reported.

Keywords

Internal Medicine Metabolic Disease Muscular Dystrophy Duchenne Muscular Dystrophy Rare Polymorphism 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

References

  1. Murray JM, Davies KE, Harper PS, Meredith L, Mueller CR, Williamson R (1982) Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne uscular dystrophy. Nature (London) 300:69–71Google Scholar
  2. Wapenaar MC, Kievits T, Hart KA, Abbs S, Blonden LAJ, Dunnen JT den, Grootscholten PM, Bakker E, Verellen-Dumoulin C, Bobrow M, Ommen GJB van, Pearson PL (1988) A deletion hot spot in the Duchenne muscular dystrophy gene. Genomics 2:101–108Google Scholar

Copyright information

© Springer-Verlag 1992

Authors and Affiliations

  • S. Uhlhaas
    • 1
  • E. Bakker
    • 2
  • C. van Broeckhoven
    • 3
  • A. Barth-Schulz
    • 4
  • W. Friedl
    • 1
  1. 1.Institut für Humangenetik der UniversitätBonnFederal Republic of Germany
  2. 2.Department of Human GeneticsLeiden University, Sylvius LaboratoryAL LeidenThe Netherlands
  3. 3.Department of BiochemistryUniversity of AntwerpWilrijkBelgium
  4. 4.Institut für Humangenetik der UniversitätFrankfurt/MFederal Republic of Germany

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